Wolfram syndrome (section WFS1)
syndrome 1 (WFS1), and Wolfram syndrome 2 (WFS2). The WFS1 or wolframin gene provides instructions for making the wolframin protein. The WFS1 gene is active...
42 KB (5,032 words) - 18:51, 17 July 2025
Wolframin is a protein that in humans is encoded by the WFS1 gene. This gene encodes a transmembrane protein, which is located primarily in the endoplasmic...
9 KB (1,173 words) - 18:50, 17 July 2025
affected with the autosomal recessive Wolfram syndrome. It is a type of WFS1-related disorder. Individuals with Wolfram-like syndrome usually exhibit...
23 KB (2,430 words) - 18:59, 16 July 2025
ubiquitin specific peptidase 53 UTP3: small subunit processome component VPS54 WFS1: Wolfram syndrome 1 (wolframin) ZGRF1: zinc-finger GRF-type containing 1...
31 KB (1,931 words) - 05:25, 19 July 2025
OTOF, PCDH15, POU3F4, SLC26A4, STRC, TECTA, TMC1, TMIE, TMPRSS3, USH1C, and WFS1 genes cause nonsyndromic deafness, with weaker evidence currently implicating...
20 KB (1,853 words) - 18:06, 16 July 2025
Q8IUB5 18310 WFIKKN1 HGNC:30912 Q96NZ8 18311 WFIKKN2 HGNC:30916 Q8TEU8 18312 WFS1 HGNC:12762 O76024 18313 WHAMM HGNC:30493 Q8TF30 18314 WHRN HGNC:16361 Q9P202...
242 KB (17 words) - 18:43, 6 October 2024
associated with type 2 diabetes, including TCF7L2, PPARG, FTO, KCNJ11, NOTCH2, WFS1, IGF2BP2, SLC30A8, JAZF1, HHEX, DGKB, CDKN2A, CDKN2B, KCNQ1, HNF1A, HNF1B...
19 KB (2,339 words) - 11:46, 19 November 2024
syndrome 2; 604928; CISD2 Wolfram syndrome; 222300; WFS1 Wolfram-like syndrome, autosomal dominant; 222300; WFS1 Wolman disease; 278000; LIPA Woodhouse–Sakati...
234 KB (18,877 words) - 18:07, 24 March 2025